A Comparative Study of the Metabolism of 6-Methylbenzo [A] Pyrene and Benzo [A] Pyrene by Rat Liver Microsomes

Abstract

In several types of carcinogenicity studies, 6-methylbenzo[a]- pyrene (6-MBaP) was found to be moderately active as a tumorigen, although with potency less than that of benzo[a]pyrene (BaP). BaP is metabolically converted to an ultimate carcinogen, the BaP (+)-trans-7,8-diol 9,10-epoxide, by an activation pathway that proceeds via a (-)-trans-7,8-diol metabolite intermediate. It has not been established if 6-MBaP is activated by a similar pathway, and alternative mechanisms for the bioactivation of 6-MBaP have been proposed which involve reactive species other than a diol epoxide. The major goal of this study was to determine the effect of methyl substitution at position six on the in vitro metabolism of 6-MBaP relative to that of BaP in order to better understand the molecular basis for differences in the biological activities of the two compounds.

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Document Details

Document Type
Technical Report
Publication Date
Feb 24, 1984
Accession Number
AD1010710

Entities

People

  • Karen L. Hamernik

Organizations

  • Uniformed Services University of the Health Sciences

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • Aromatic Hydrocarbons
  • Chemical Synthesis
  • Chemistry
  • Chromatography
  • Enantiomers
  • Endoplasmic Reticulum
  • Health Services
  • Hydrocarbons
  • Isomers
  • Liquid Chromatography
  • Magnetic Resonance
  • Mass Spectroscopy
  • Materials
  • Molecules
  • Nuclear Magnetic Resonance
  • Organic Chemistry
  • Spectroscopy

Readers

  • Analytical Chemistry
  • Molecular Genetics
  • Toxicology/Environmental Toxicology